Canonical Allele Identifier: PA2825167052
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1929389
ClinVar RCV Id: RCV002642362
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000417.3:p.Thr617Arg
CA365609612
NM_000426.4:c.1850C>G